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Tumefactive multiple sclerosis requiring emergent biopsy and histological investigation to confirm the diagnosis: a case report

机译:Tumefactive多发性硬化症,需要紧急活检和组织学检查以确认诊断:病例报告

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Introduction Tumefactive multiple sclerosis is a demyelinating disease that demonstrates tumor-like features on magnetic resonance imaging. Although diagnostic challenges without biopsy have been tried by employing radiological studies and cerebrospinal fluid examinations, histological investigation is still necessary for certain diagnosis in some complicated cases. Case presentation A 37-year-old Asian man complaining of mild left leg motor weakness visited our clinic. Magnetic resonance imaging demonstrated high-signal lesions in bilateral occipital forceps majors, the left caudate head, and the left semicentral ovale on fluid-attenuated inversion recovery and T2-weighted imaging, and these lesions were enhanced by gadolinium-dimeglumin. Tumefactive multiple sclerosis was suspected because the enhancement indistinctly extended along the corpus callosum on magnetic resonance imaging and scintigraphy showed a low malignancy of the lesions. But oligoclonal bands were not detected in cerebrospinal fluid. In a few days, his symptoms fulminantly deteriorated with mental confusion and left hemiparesis, and steroid pulse therapy was performed. In spite of the treatment, follow-up magnetic resonance imaging showed enlargement of the lesions. Therefore, emergent biopsy was performed and finally led to the diagnosis of demyelinating disease. The enhanced lesion on magnetic resonance imaging disappeared after one month of prednisolone treatment, but mild disorientation and left hemiparesis remained as sequelae. Conclusions Fulminant aggravation of the disease can cause irreversible neurological deficits. Thus, an early decision to perform a biopsy is necessary for exact diagnosis and appropriate treatment if radiological studies and cerebrospinal fluid examinations cannot rule out the possibility of brain tumors.
机译:简介Tumefactive多发性硬化症是一种脱髓鞘疾病,在磁共振成像中表现出肿瘤样特征。尽管已经通过放射学研究和脑脊液检查尝试了无活检的诊断挑战,但在某些复杂病例中,对于某些诊断仍需进行组织学检查。病例介绍一名37岁的亚洲男子抱怨轻度左腿运动无力前往我们的诊所。磁共振成像显示双侧枕骨钳大动脉,左尾状头和左半中卵圆形的高信号病变在液衰减倒置恢复和T2加权成像上,并且lesions-二聚球蛋白增强了这些病变。怀疑有Tumefactive型多发性硬化症,因为在磁共振成像和闪烁显像术显示病变的恶性程度较低时,增强作用沿along体模糊延伸。但是在脑脊液中未检测到寡克隆带。几天后,他的症状因精神错乱和左偏瘫而急剧恶化,并进行了类固醇脉冲治疗。尽管进行了治疗,但后续的磁共振成像显示病变增大。因此,进行了活检,最终导致脱髓鞘疾病的诊断。泼尼松龙治疗一个月后,磁共振成像上增强的病变消失,但轻度迷失方向和左偏瘫仍为后遗症。结论该病的严重加重可引起不可逆的神经功能缺损。因此,如果放射学研究和脑脊液检查不能排除脑瘤的可能性,则必须尽早决定进行活检以进行准确的诊断和适当的治疗。

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